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dc.contributor.authorSadıkov, N
dc.contributor.authorNasibov, A
dc.contributor.authorÖğretir, Cemil
dc.contributor.authorBerber, Halil
dc.contributor.authorHüseyinli, A
dc.date.accessioned2019-10-20T09:30:50Z
dc.date.available2019-10-20T09:30:50Z
dc.date.issued2004
dc.identifier.issn1420-3049
dc.identifier.urihttps://dx.doi.org/10.3390/91100922
dc.identifier.urihttps://hdl.handle.net/11421/17483
dc.descriptionWOS: 000227831900003en_US
dc.descriptionPubMed ID: 18007493en_US
dc.description.abstractThe alkylation of beta-dicarbonyl compounds in a K2CO3/DMSO system was found to afford O- and C-alkylated derivatives, depending on the type of the P-dicarbonyl compound involved. The alkyl derivatives obtained were used in the synthesis of some new spiro barbituric acid derivatives. Quantum chemical calculations were carried out to elucidate the reaction mechanisms for some typical synthesis.en_US
dc.language.isoengen_US
dc.publisherMDPIen_US
dc.relation.isversionof10.3390/91100922en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAlkylation Of Beta-Dicarbonyl Compoundsen_US
dc.subjectSpiro Derivatives Of Barbituric Aciden_US
dc.subject2-Chloro-1-(2-Chloroethoxy)Ethaneen_US
dc.subjectTheoretical Studiesen_US
dc.titleQuantum chemical and experimental studies on the mechanism of alkylation of beta-dicarbonyl compounds. The synthesis of five and six membered heterocyclic spiro derivativesen_US
dc.typearticleen_US
dc.relation.journalMoleculesen_US
dc.contributor.departmentAnadolu Üniversitesi, Fen Fakültesi, Fizik Bölümüen_US
dc.identifier.volume9en_US
dc.identifier.issue11en_US
dc.identifier.startpage922en_US
dc.identifier.endpage938en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.contributor.institutionauthorBerber, Halil


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